rs1057519607

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs1057519607(-;C)

Make rs1057519607(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

18178849

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs1057519607
dbSNP (classic)	rs1057519607
ClinGen	rs1057519607
ebi	rs1057519607
HLI	rs1057519607
Exac	rs1057519607
Gnomad	rs1057519607
Varsome	rs1057519607
LitVar	rs1057519607
Map	rs1057519607
PheGenI	rs1057519607
Biobank	rs1057519607
1000 genomes	rs1057519607
hgdp	rs1057519607
ensembl	rs1057519607
geneview	rs1057519607
scholar	rs1057519607
google	rs1057519607
pharmgkb	rs1057519607
gwascentral	rs1057519607
openSNP	rs1057519607
23andMe	rs1057519607
SNPshot	rs1057519607
SNPdbe	rs1057519607
MSV3d	rs1057519607
GWAS Ctlg	rs1057519607

Max Magnitude

0

ClinVar
Risk	rs1057519607(C;C)
Alt	rs1057519607(C;C)
Reference	Rs1057519607(-;-)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO15A
CLNDBN	Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18082163dupC
CLNSRC
CLNACC	RCV000417125.1,